HGVS | Genome Assembly |
---|---|
NC_000019.10:g.40845080T>A , CM000681.2:g.40845080T>A | GRCh38 |
NC_000019.9:g.41350985T>A , CM000681.1:g.41350985T>A | GRCh37 |
NC_000019.8:g.46042825T>A | NCBI36 |
NG_008377.1:g.10368A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000301141.10:c.1161+214A>T MANE Select | ENSP00000301141.4:n.1161+214A>T | |
ENST00000301141.9:c.1161+214A>T | ENSP00000301141.4:n.1161+214A>T | |
ENST00000596719.5:n.1226A>T | ||
ENST00000601627.1:c.119+43665T>A | ||
ENST00000610301.1:c.1161+214A>T | ENSP00000477899.1:n.1161+214A>T | |
NM_000762.5:c.1161+214A>T | NP_000753.3:n.1161+214A>T | |
NM_000762.6:c.1161+214A>T MANE Select | NP_000753.3:n.1161+214A>T |